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Treatment of Alcohols with Tosyl Chloride Does Not always Lead to the Formation of Tosylates

Treatment of substituted benzyl alcohols with tosyl chloride resulted in the formation of the corresponding chlorides, not the usual tosylates. A series of experiments demonstrated that it was possible to predict whether chlorination or tosylation would occur for substituted benzyl alcohols and pyri...

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Detalles Bibliográficos
Autores principales: Ding, Rui, He, Yong, Wang, Xiao, Xu, Jingli, Chen, Yurong, Feng, Man, Qi, Chuanmin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264569/
https://www.ncbi.nlm.nih.gov/pubmed/21725279
http://dx.doi.org/10.3390/molecules16075665
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author Ding, Rui
He, Yong
Wang, Xiao
Xu, Jingli
Chen, Yurong
Feng, Man
Qi, Chuanmin
author_facet Ding, Rui
He, Yong
Wang, Xiao
Xu, Jingli
Chen, Yurong
Feng, Man
Qi, Chuanmin
author_sort Ding, Rui
collection PubMed
description Treatment of substituted benzyl alcohols with tosyl chloride resulted in the formation of the corresponding chlorides, not the usual tosylates. A series of experiments demonstrated that it was possible to predict whether chlorination or tosylation would occur for substituted benzyl alcohols and pyridine methanols. Treatment of electron withdrawing group-substituted benzyl alcohols with tosyl chloride gave the corresponding chlorides in moderate yields under mild conditions, which provided a simple way to directly prepare chlorides from alcohols.
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spelling pubmed-62645692018-12-10 Treatment of Alcohols with Tosyl Chloride Does Not always Lead to the Formation of Tosylates Ding, Rui He, Yong Wang, Xiao Xu, Jingli Chen, Yurong Feng, Man Qi, Chuanmin Molecules Article Treatment of substituted benzyl alcohols with tosyl chloride resulted in the formation of the corresponding chlorides, not the usual tosylates. A series of experiments demonstrated that it was possible to predict whether chlorination or tosylation would occur for substituted benzyl alcohols and pyridine methanols. Treatment of electron withdrawing group-substituted benzyl alcohols with tosyl chloride gave the corresponding chlorides in moderate yields under mild conditions, which provided a simple way to directly prepare chlorides from alcohols. MDPI 2011-07-01 /pmc/articles/PMC6264569/ /pubmed/21725279 http://dx.doi.org/10.3390/molecules16075665 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Ding, Rui
He, Yong
Wang, Xiao
Xu, Jingli
Chen, Yurong
Feng, Man
Qi, Chuanmin
Treatment of Alcohols with Tosyl Chloride Does Not always Lead to the Formation of Tosylates
title Treatment of Alcohols with Tosyl Chloride Does Not always Lead to the Formation of Tosylates
title_full Treatment of Alcohols with Tosyl Chloride Does Not always Lead to the Formation of Tosylates
title_fullStr Treatment of Alcohols with Tosyl Chloride Does Not always Lead to the Formation of Tosylates
title_full_unstemmed Treatment of Alcohols with Tosyl Chloride Does Not always Lead to the Formation of Tosylates
title_short Treatment of Alcohols with Tosyl Chloride Does Not always Lead to the Formation of Tosylates
title_sort treatment of alcohols with tosyl chloride does not always lead to the formation of tosylates
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264569/
https://www.ncbi.nlm.nih.gov/pubmed/21725279
http://dx.doi.org/10.3390/molecules16075665
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